A novel epithelial sodium channel β-subunit mutation associated with hypertensive Liddle syndrome

Pediatric Nephrology

Volumn 20, Issue 4, 2005, Pages 512-515

  Freundlich, Michael ^a,c   Ludwig, Michael ^b  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF BONN   (Germany)

^c Pediatric Specialty Center   (United States)

Author keywords

Aldosterone; Blood pressure; Hypertension; Hypokalemia; Renin

Indexed keywords

ALDOSTERONE; AMILORIDE; HYDROCHLOROTHIAZIDE; RENIN; SODIUM CHANNEL; STEROID;

ARTICLE; BLOOD PRESSURE REGULATION; CASE REPORT; DIAGNOSTIC ACCURACY; DIASTOLIC BLOOD PRESSURE; DNA DETERMINATION; DRUG DOSE REGIMEN; EPITHELIUM; FEMALE; GENE MUTATION; HETEROZYGOSITY; HUMAN; HYPERTENSION; LIDDLE SYNDROME; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SODIUM RESTRICTION; STEROID URINE LEVEL; SYSTOLIC BLOOD PRESSURE;

AMILORIDE; AMINO ACID SUBSTITUTION; BASE SEQUENCE; CHILD, PRESCHOOL; DIURETICS; DRUG THERAPY, COMBINATION; EPITHELIAL SODIUM CHANNEL; FEMALE; HETEROZYGOTE; HISTIDINE; HUMANS; HYDROCHLOROTHIAZIDE; HYPERTENSION; MUTATION; PROLINE; PROTEIN ISOFORMS; PSEUDOHYPOALDOSTERONISM; RENIN; SODIUM CHANNELS; SODIUM CHLORIDE SYMPORTER INHIBITORS;

EID: 15344340558     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-004-1751-2     Document Type: Article

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